A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053894



Internal ID18796425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30077711..30796262hg38UCSC Ensembl
Innerchr15:30369914..31088465hg19UCSC Ensembl
Innerchr15:28157206..28875757hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38718552
hg19718552
hg18718552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2496n100
Supporting Variantsnssv3545683, nssv3545682
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053894
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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